DRI — Monitor, Line Isolation Class I
FDA Device Classification
Classification Details
- Product Code
- DRI
- Device Class
- Class I
- Regulation Number
- 870.2620
- Submission Type
- Review Panel
- CV
- Medical Specialty
- Cardiovascular
- Implant
- No
Recent 510(k) Clearances
| K-Number | Applicant | Device Name | Date |
|---|
| K902493 | datex division instrumentarium | CARDIOCAP II CG-2GS, 2G, 1GS, 1G, 2CG, CS MONITOR | July 6, 1990 |
| K902492 | datex division instrumentarium | CARDIOCAP II MONITORS: CH, CH-2, CH-S, CH-2S | July 6, 1990 |
| K822316 | hmba | HEART MONITOR BRACELET ALARM | September 21, 1982 |
| K802326 | stanco medical | PRESSURE MONITORING LINES | October 10, 1980 |